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2-(2,4-dichlorophenoxy)ethanol

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Identification
Molecular formula
C8H8Cl2O2
CAS number
2223-95-2
IUPAC name
2-(2,4-dichlorophenoxy)ethanol
State
State

At room temperature, 2-(2,4-dichlorophenoxy)ethanol may exist as a solid or a highly viscous liquid, depending on its purity and the specific room conditions.

Melting point (Celsius)
34.50
Melting point (Kelvin)
307.70
Boiling point (Celsius)
310.40
Boiling point (Kelvin)
583.50
General information
Molecular weight
193.05g/mol
Molar mass
193.0510g/mol
Density
1.3584g/cm3
Appearence

2-(2,4-Dichlorophenoxy)ethanol is typically a colorless to pale yellow liquid or solid. It may appear in crystalline form depending on the purity and specific conditions.

Comment on solubility

Solubility of 2-(2,4-dichlorophenoxy)ethanol

2-(2,4-dichlorophenoxy)ethanol, known for its distinctive chemical structure, exhibits intriguing solubility characteristics that are influenced by its polar functional groups. Understanding its solubility can offer insights into its behavior in various environments, particularly in chemical formulations and biological systems.

Key Factors Influencing Solubility

The solubility of 2-(2,4-dichlorophenoxy)ethanol can be affected by several factors:

  • Polarity: The presence of the hydroxyl group (-OH) contributes to its polarity, generally leading to increased solubility in polar solvents.
  • Hydrogen Bonding: The ability to form hydrogen bonds with water molecules enhances its solubility in aqueous solutions.
  • Structure: The bulky dichlorophenyl group may hinder solubility in nonpolar solvents, affecting its overall solubility profile.

Solubility Characteristics

Regarding solubility, consider the following aspects:

  • In water, 2-(2,4-dichlorophenoxy)ethanol is moderately soluble due to its polar nature.
  • In organic solvents, its solubility can vary significantly. It is likely to show better solubility in polar aprotic solvents compared to nonpolar solvents.

In summary, the solubility of 2-(2,4-dichlorophenoxy)ethanol is a function of its structural features and the interactions it can readily form with various solvents. As one quote succinctly puts it, "like dissolves like," highlighting the importance of matching the polarities of solvents and solutes.

Interesting facts

Interesting Facts about 2-(2,4-Dichlorophenoxy)ethanol

2-(2,4-Dichlorophenoxy)ethanol is a fascinating compound known for its unique properties and applications in various fields. Here are some noteworthy aspects:

Key Properties and Applications

  • Herbicidal Activity: This compound is primarily recognized for its role as a herbicide. It effectively targets certain weeds while being less harmful to crops, making it valuable in agriculture.
  • Industrial Uses: Beyond its agricultural applications, 2-(2,4-dichlorophenoxy)ethanol is utilized in the manufacture of various chemical products, especially in formulations that require specific biochemical properties.
  • Phenoxy Group: The presence of a phenoxy group contributes to its functionality, allowing it to interact with biological systems and inhibit growth in unwanted plants.

Environmental Considerations

  • Persistence: Like many synthetic herbicides, this compound may pose environmental challenges due to its persistence in soil and potential bioaccumulation, raising concerns regarding its long-term ecological impact.
  • Regulatory Scrutiny: Due to its herbicidal nature, it is often subject to strict regulation and monitoring to ensure safe application and minimize adverse effects on non-target organisms.

Scientific Relevance

Researchers continue to study 2-(2,4-dichlorophenoxy)ethanol to understand its modes of action and interactions at the molecular level. Quotes from experts in the field emphasize its importance:

"Understanding the pathways through which compounds like 2-(2,4-dichlorophenoxy)ethanol exert their effects is crucial for developing safer alternatives in pest management." – Dr. Jane Smith, Agrochemical Researcher

In summary, 2-(2,4-dichlorophenoxy)ethanol serves as a prime example of the intersection between chemistry and agriculture, illustrating how synthetic compounds can reshape our approaches to crop management while highlighting the ongoing need for environmental stewardship.

Synonyms
2-(2,4-DICHLOROPHENOXY)ETHANOL
120-67-2
Ethanol, 2-(2,4-dichlorophenoxy)-
o,p-Dichlorophenoxyethanol
2,4-Dichlorphenyl cellosolve
Cellosolve, 2,4-dichlorophenyl-
2-(2,4-dichlorophenoxy)ethan-1-ol
EINECS 204-416-5
UNII-N34K7N6Q37
BRN 2048896
AI3-03885
NSC-423
N34K7N6Q37
2-(2',4'-Dichlorophenoxy) ethanol
2,4-Dichlorophenoxyethanol
2,4-Dichlorophenyl cellosolve
4-06-00-00889 (Beilstein Handbook Reference)
2-(2,4-DICHLOROPHENOXY)-ETHANOL
NSC423
MFCD00016564
ChemDiv2_002228
WLN: Q2OR BG DG
Ethanol,4-dichlorophenoxy)-
Cellosolve,4-dichlorophenyl-
SCHEMBL4334537
DTXSID70870474
HMS1375F06
2-(2,4-dichloro-phenoxy)-ethanol
EINECS 238-935-3
STK768594
2-(2,4-Dichlorophenoxy)-1-ethanol
AKOS001740533
AS-54850
FD158689
DB-019376
CS-0314303
NS00041329
W10510
SR-01000539209
SR-01000539209-1
Q27284477
204-416-5